材料科学
镍
电池(电)
阴极
离子
能量色散X射线光谱学
过渡金属
氧化物
电极
降级(电信)
冶金
化学工程
扫描电子显微镜
复合材料
电子工程
物理化学
功率(物理)
有机化学
化学
催化作用
工程类
物理
量子力学
生物化学
作者
Dong‐Su Ko,Jun‐Ho Park,Byong Yong Yu,Docheon Ahn,Kihong Kim,Heung Nam Han,Woo Sung Jeon,Changhoon Jung,Arumugam Manthiram
标识
DOI:10.1002/aenm.202001035
摘要
Abstract Multiple applications of lithium‐ion batteries in energy storage systems and electric vehicles require highly stable electrode materials for long‐term battery operation. Among the various cathode materials, high‐Ni cathode materials enable a high energy density. However, cathode degradation accompanied by complex chemical and structural changes results in capacity and voltage fading in batteries. Cathode degradation remains poorly understood; the majority of studies have only explored the oxidation states of transition‐metal ions in localized areas and have rarely evaluated chemical degradation in complete particles after prolonged cycling. This study systematically investigates the degradation of a high‐Ni cathode by comparing the chemical, structural, and electrical changes in pristine and 500 times‐cycled cathodes. Electron probe micro‐analysis and X‐ray energy dispersive spectroscopy reveal changes in the Ni:O ratio from 1:2 to 1:1 over a large area inside the secondary particle. Electron energy loss spectroscopy analysis related to structural changes is performed for the entire primary particle area to visualize the oxidation state of transition‐metal ions in two dimensions. The results imply that the observed monotonic capacity fade without unusual changes is due to the continuous formation of the Ni 2+ phase from the surface to the bulk through chemical and structural degradation.
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